Clinical research - senior sas programmers jobs in cambridgeshir

Cambridgeshire

clinical research - senior sas programmer job in the cambridge area salary - highly attractive salary + excellent benefits package flame pharma are working with a leading global contract research organization providing discovery and development services and drug lifecycle management. with an enviable client base across pharmaceutical, biotechnology, medical device, academic and government organizations, this organisation are able to offer long term opportunities[...]

Job Type: Permanent

26/05/2012 08:00 » CareerBuilder » Cambridgeshire | East of England 

Senior drug safety specialist - cambridgeshire

Cambridgeshire

[...] contract research organisations (cros). i-pharm has specific expertise in clinical research, medical affairs, regulatory affairs, pharmacovigilance, quality assurance and bioinformatics. www.i-pharmconsulting.com to apply if you would like to discuss this vacancy further, please call pharmacovigilance recruitment consultant on +44 (0)20 3189 2299, or email jbalfour@i-pharmconsulting.com. if this role is not suitable, joe is also available to discuss other[...]

Job Type: Permanent

23/05/2012 16:00 » EuroJobs » Cambridgeshire | East of England 

Software engineer

CK Group — Cambridgeshire

[...] and clinical research to medical information. we strive to deliver a world class service through our separate tailored divisions: ck science is the leading independent scientific recruitment consultancy in the uk. ck clinical is an established leader in the clinical research and drug development sectors. ck eu pharma jobs concentrates on recruitment for pharmaceutical jobs in mainland europe. ck it specialises in jobs for it professionals working[...]

23/05/2012 15:00 » Monster » Cambridgeshire | East of England 

Mechanical design engineer - cambridgeshire

CK Group - — Cambridgeshire

[...] and clinical research to medical information. we strive to deliver a world class service through our separate tailored divisions: ck science is the leading independent scientific recruitment consultancy in the uk. ck clinical is an established leader in the clinical research and drug development sectors. ck eu pharma jobs concentrates on recruitment for pharmaceutical jobs in mainland europe. ck it specialises in jobs for it professionals working[...]

22/05/2012 11:00 » Monster » Cambridgeshire | East of England 

Drug safety associate (uk)

Cambridgeshire

[...] form clinical trials and post marketing sources onto our global safety database (arisg), in accordance with sops and regulatory requirements. 2.assisting with sae reconciliation 3.end user of safety databases and case narrative writing 4.contributing to the on going enhancement of pharmacovigilance processes and writing standard operating procedures. 5.supporting the pharmacovigilance team with the creation and quality control of safety reports in csrs, dsur/psurs, and[...]

Job Type: Permanent

17/05/2012 12:00 » EuroJobs » Cambridgeshire | East of England 

Drug safety specialist ii

Cambridgeshire

[...] contract research organisations (cros). i-pharm has specific expertise in clinical research, medical affairs, regulatory affairs, pharmacovigilance, quality assurance and bioinformatics. www.i-pharmconsulting.com to apply if you would like to discuss this vacancy further, please call pharmacovigilance recruitment consultant on +44 (0)20 3189 2299, or email jbalfour@i-pharmconsulting.com. if this role is not suitable, joe is also available to discuss other[...]

Job Type: Permanent

17/05/2012 11:00 » EuroJobs » Cambridgeshire | East of England 

Clinical project manager - clinical pm - cambridge

Cambridgeshire

clinical project manager - clinical pm - cambridgeshire - clinical research would you like to work for a company that praise you for doing well rather than just pointing out your faults? an exciting opportunity has arisen to join a small but well established clinical research organisation based in cambridgeshire for a clinical project manager. this fantastic company are looking for an experienced clinical project manager to[...]

Job Type: Permanent

14/05/2012 14:00 » EuroJobs » Cambridgeshire | East of England 

Senior regulatory affairs associate

Cambridgeshire

[...] of non-clinical, clinical and safety regulatory documentation in accordance with regulations, post licensing commitments and legal obligations. *provide advice and practical input on labelling issues across the development and marketed product portfolio. *assist more junior personnel in completing tasks. requirements: 1.bachelor's degree in biological/life sciences. 2.around 3 years experience within regulatory affairs 3.experience in the preparation/submission of[...]

Job Type: Permanent

11/05/2012 16:00 » EuroJobs » Cambridgeshire | East of England 

Safety specialist (contract)

Cambridgeshire

[...] contract research organisations (cros). i-pharm has specific expertise in clinical research, medical affairs, regulatory affairs, pharmacovigilance, quality assurance and bioinformatics. www.i-pharmconsulting.com to apply if you would like to discuss this vacancy further, please call consultant joe balfour on +44 (0)20 3189 2299, or email jbalfour@i-pharmconsulting.com. if this role is not suitable, joe is also available to discuss other possible positions[...]

Job Type: Permanent

11/05/2012 10:00 » EuroJobs » Cambridgeshire | East of England 

Regulatory affairs executive - east anglia

Cambridgeshire

[...] stage clinical research to the pharmaceutical industry. as the regulatory affairs executive you will liaise with companies, regulatory authorities and internal departments and be responsible for regulatory documentation to support cta's, ind's, maa's, orphan drug applications and scientific meetings. the role reports to the regulatory affairs consultant and team leader. key responsibilities: ï §maintain regulatory awareness for strategic development ï[...]

Job Type: Permanent

11/05/2012 07:00 » EuroJobs » Cambridgeshire | East of England 

Regulatory affairs scientist

Cambridgeshire

[...] regulation: clinical/post marketing, different therapeutic areas etc. requirements 1.prior regulatory experience (1-2 years) 2.a good basis of regulatory affairs and a basic grasp of current regulations. 3.bsc/phd in a scientific discipline 4.competent in it skills including ms office 5.good written and verbal skills about i-pharm consulting i-pharm consulting is a specialist recruitment company servicing the pharmaceutical industry in the uk and europe. we provide both[...]

Job Type: Permanent

10/05/2012 18:00 » EuroJobs » Cambridgeshire | East of England 

Regulatory affairs associate (contract), uk

Cambridgeshire

[...] submit clinical trial applications, amendments and end of trial applications. *prepare type i/ii variations *reviewing and approving non-promotional meeting venues, hospitality events and contracts and meeting agenda. *liaise with several groups within the company and to be able to submit and qualify information to these groups. requirements 1.knowledge of uk and ireland regulations 2.have experience of regulatory submissions and knowledge of the regulatory framework. 3[...]

Job Type: Temporary/Contract/Project

08/05/2012 14:00 » EuroJobs » Cambridgeshire | East of England 

Clinical project manager - cambridgeshire

Cambridgeshire

[...] lead clinical research associate (lcra) or clinical project manager (cpm). my client prides themselves on being experts in early phase clinical research (i&ii) trials, with a strong focus on oncology, renal and neurology studies. at present we search for an experienced clinical project manager that would benefit from sharing their expertise within an intimate team of clinical professionals and seeing a footprint of how one has[...]

Job Type: Permanent

06/05/2012 21:00 » EuroJobs » Cambridgeshire | East of England